Sindrom mačijeg plača (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sindrom mačijeg plača" in Serbian language version.

refsWebsite

Global rank Serbian rank

6doi.org

2^nd place

4^th place

4nih.gov

4^th place

8^th place

3worldcat.org

5^th place

12^th place

2semanticscholar.org

11^th place

23^rd place

1verified.rs

low place

1genome.gov

9,308^th place

9,255^th place

1bionet-skola.com

low place

1,467^th place

1betterhealth.vic.gov.au

low place

betterhealth.vic.gov.au

„Cri du chat syndrome - Better Health Channel”. www.betterhealth.vic.gov.au. Приступљено 2022-02-16.

bionet-skola.com

Trifunović, Snežana. „Sindrom mačijeg plača”. www.bionet-skola.com. Приступљено 16. 2. 2022.

doi.org

Sheth, Frenny; Gohel, Naresh; Liehr, Thomas; Akinde, Olakanmi; Desai, Manisha; Adeteye, Olawaleye; Sheth, Jayesh (2012). „Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome”. Case Reports in Genetics. 2012: 153405. ISSN 2090-6544. PMC 3539376 . PMID 23320207. doi:10.1155/2012/153405 .
Rinaldi, R.; De Bernardo, C.; Assumma, M.; Grammatico, B.; Buffone, E.; Poscente, M.; Grammatico, P. (2003-02-10). „Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype”. American Journal of Medical Genetics Part A. 118A (2): 122—126. ISSN 1552-4825. doi:10.1002/ajmg.a.10093.
Sanders, Catherine D.; Leigh, Margaret W.; Chao, Kay C.; Weck, Karen E.; King, Ian; Wolf, Whitney E.; Campbell, Dennis J.; Knowles, Michael R.; Zariwala, Maimoona A.; Shapiro, Adam J. (2018). „The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort”. Pediatr Pulmonol. 53 (11): 1565—73. PMID 30238669. S2CID 52309122. doi:10.1002/ppul.24159. .
Cerruti Mainardi, Paola (2006-09-05). „Cri du Chat syndrome”. Orphanet Journal of Rare Diseases. 1: 33. ISSN 1750-1172. PMC 1574300 . PMID 16953888. doi:10.1186/1750-1172-1-33 .
Pizzamiglio, M. R.; Nasti, M.; Piccardi, L.; Vitturini, C.; Morelli, D.; Guariglia, C. (2008). „Visual-motor coordination computerized training improves the visuo-spatial performance in a child affected by Cri-du-Chat syndrome”. Int J Rehabil Res. 31 (2): 151—4. PMID 18467929. S2CID 205864451. doi:10.1097/MRR.0b013e3282fbfbde. .

dx.doi.org

Rinaldi, R.; De Bernardo, C.; Assumma, M.; Grammatico, B.; Buffone, E.; Poscente, M.; Grammatico, P. (2003-02-10). „Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype”. American Journal of Medical Genetics Part A. 118A (2): 122—126. ISSN 1552-4825. doi:10.1002/ajmg.a.10093.

genome.gov

„About Cri du Chat Syndrome”. Genome.gov (на језику: енглески). Приступљено 2022-02-16.

nih.gov

ncbi.nlm.nih.gov

Sheth, Frenny; Gohel, Naresh; Liehr, Thomas; Akinde, Olakanmi; Desai, Manisha; Adeteye, Olawaleye; Sheth, Jayesh (2012). „Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome”. Case Reports in Genetics. 2012: 153405. ISSN 2090-6544. PMC 3539376 . PMID 23320207. doi:10.1155/2012/153405 .
Sanders, Catherine D.; Leigh, Margaret W.; Chao, Kay C.; Weck, Karen E.; King, Ian; Wolf, Whitney E.; Campbell, Dennis J.; Knowles, Michael R.; Zariwala, Maimoona A.; Shapiro, Adam J. (2018). „The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort”. Pediatr Pulmonol. 53 (11): 1565—73. PMID 30238669. S2CID 52309122. doi:10.1002/ppul.24159. .
Cerruti Mainardi, Paola (2006-09-05). „Cri du Chat syndrome”. Orphanet Journal of Rare Diseases. 1: 33. ISSN 1750-1172. PMC 1574300 . PMID 16953888. doi:10.1186/1750-1172-1-33 .
Pizzamiglio, M. R.; Nasti, M.; Piccardi, L.; Vitturini, C.; Morelli, D.; Guariglia, C. (2008). „Visual-motor coordination computerized training improves the visuo-spatial performance in a child affected by Cri-du-Chat syndrome”. Int J Rehabil Res. 31 (2): 151—4. PMID 18467929. S2CID 205864451. doi:10.1097/MRR.0b013e3282fbfbde. .

semanticscholar.org

api.semanticscholar.org

Sanders, Catherine D.; Leigh, Margaret W.; Chao, Kay C.; Weck, Karen E.; King, Ian; Wolf, Whitney E.; Campbell, Dennis J.; Knowles, Michael R.; Zariwala, Maimoona A.; Shapiro, Adam J. (2018). „The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort”. Pediatr Pulmonol. 53 (11): 1565—73. PMID 30238669. S2CID 52309122. doi:10.1002/ppul.24159. .
Pizzamiglio, M. R.; Nasti, M.; Piccardi, L.; Vitturini, C.; Morelli, D.; Guariglia, C. (2008). „Visual-motor coordination computerized training improves the visuo-spatial performance in a child affected by Cri-du-Chat syndrome”. Int J Rehabil Res. 31 (2): 151—4. PMID 18467929. S2CID 205864451. doi:10.1097/MRR.0b013e3282fbfbde. .

verified.rs

„Šta su mikrodelecije?”. Prenatalni test - Verified (на језику: енглески). 2019-04-25. Приступљено 2022-02-16.

worldcat.org

Sheth, Frenny; Gohel, Naresh; Liehr, Thomas; Akinde, Olakanmi; Desai, Manisha; Adeteye, Olawaleye; Sheth, Jayesh (2012). „Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome”. Case Reports in Genetics. 2012: 153405. ISSN 2090-6544. PMC 3539376 . PMID 23320207. doi:10.1155/2012/153405 .
Rinaldi, R.; De Bernardo, C.; Assumma, M.; Grammatico, B.; Buffone, E.; Poscente, M.; Grammatico, P. (2003-02-10). „Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype”. American Journal of Medical Genetics Part A. 118A (2): 122—126. ISSN 1552-4825. doi:10.1002/ajmg.a.10093.
Cerruti Mainardi, Paola (2006-09-05). „Cri du Chat syndrome”. Orphanet Journal of Rare Diseases. 1: 33. ISSN 1750-1172. PMC 1574300 . PMID 16953888. doi:10.1186/1750-1172-1-33 .